Quantification of surrogate monoclonal antibodies in mouse serum using LC–MS/MS

Author:

Mehl John T1ORCID,Landry France1,Discenza Lorell1,Sleczka Bogdan1,Zhao Qihong2,Shuster David J3,Madia Priyanka4,DasGupta Ruchira5,Rajendran Surendran6,Sun Huadong7,Ciccimaro Eugene8,Olah Timothy V9

Affiliation:

1. Bioanalytical Research, Bristol Myers Squibb, Princeton, NJ, USA

2. Discovery Biology, Bristol Myers Squibb, Princeton, NJ, USA

3. Veterinary Sciences, Bristol Myers Squibb, Princeton, NJ, USA

4. Metabolism & Pharmacokinetics, Bristol Myers Squibb, Princeton, NJ, USA

5. Biomolecular Characterization, Bristol Myers Squibb, Cambridge, MA, USA

6. Bioanalytical Sciences, Bristol Myers Squibb, Princeton, NJ, USA

7. Sarepta Therapeutic Inc, Cambridge, MA, USA

8. Agilent Technologies, Wilmington, DE, USA

9. Independent Consultant, Pennington, NJ, USA

Abstract

Background: Surrogate monoclonal antibodies (mAbs) used in preclinical in vivo studies can be challenging to quantify due to lack of suitable immunoaffinity reagents or unavailability of the mAb protein sequence. Generic immunoaffinity reagents were evaluated to develop sensitive LC–MS/MS assays. Peptides of unknown sequence can be used for selective LC–MS quantification. Results: anti-mouse IgG1 was found to be an effective immunoaffinity reagent, enabling quantification of mouse IgG1 mAbs in mouse serum. Selective peptides of unknown sequence were applied for multiplex LC–MS quantification of two rat mAbs co-dosed in mouse. Conclusion: Generic anti-mouse IgG subtype-specific antibodies can be used to improve assay sensitivity and peptides of unknown sequence can be used to quantify surrogate mAbs when the mAb protein sequence in unavailable.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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